4-Aminopyridine → 2,4,6-trichloro-N-(pyridin-4-yl)benzamide
Reaction equation
[CH:44]([N:45]([CH2:46][CH3:47])[CH:48]([CH3:49])[CH3:50])([CH3:51])[CH3:52].[Cl:1][c:2]1[c:3]([C:4](=[O:5])[OH:6])[c:7]([Cl:12])[cH:8][c:9]([Cl:11])[cH:10]1.[NH2:13][c:14]1[cH:15][cH:16][n:17][cH:18][cH:19]1.[O:53]=[CH:54][N:55]([CH3:56])[CH3:57].[P-:20]([F:21])([F:22])([F:23])([F:24])([F:25])[F:26].[n:27]1([O:28][C:29]([N:30]([CH3:31])[CH3:32])=[N+:33]([CH3:34])[CH3:35])[c:36]2[n:37][cH:38][cH:39][cH:40][c:41]2[n:42][n:43]1>>[Cl:1][c:2]1[c:3]([C:4](=[O:6])[NH:13][c:14]2[cH:15][cH:16][n:17][cH:18][cH:19]2)[c:7]([Cl:12])[cH:8][c:9]([Cl:11])[cH:10]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-3bffe99dbd9e465980194b1772f1bf3b
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
Loading…